Practice Survey on Femoral Neck Fractures and the Incidence of Type of Anesthesia on Patient Outcome
NCT ID: NCT02198820
Last Updated: 2015-06-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2014-10-31
2015-09-30
Brief Summary
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Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.
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Detailed Description
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Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.
This comparison includes preoperative parameters (hemoglobin, creatinine, mini-mental test) and intraoperative parameters (such as type of anesthesia).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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General
All patients included who underwent surgery with general anesthesia
General Anesthesia
General anesthesia with proposal, rocuronium and sufentanil
Loco Regional
All patients included who underwent surgery with loco regional anesthesia
Loco Regional Anesthesia
Loco Regional Anesthesia with marcaine
Interventions
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General Anesthesia
General anesthesia with proposal, rocuronium and sufentanil
Loco Regional Anesthesia
Loco Regional Anesthesia with marcaine
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Astes
OTHER
Responsible Party
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Eric DEFLANDRE, MD, FCCP
Eric DEFLANDRE, MD, FCCP
Principal Investigators
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Eric P DEFLANDRE, MD, FCCP
Role: PRINCIPAL_INVESTIGATOR
Astes
Locations
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Clinique Saint-Luc de Bouge
Namur, Namur, Belgium
Countries
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Other Identifiers
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FNF-SLBO
Identifier Type: -
Identifier Source: org_study_id
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